The invention relates to 5-alkyl-7-aminotriazolopyrimidines of the formula (I) and to the salts thereof. In said formula substituents have the following meanings: R1 and R2 each is a hydrogen atom or a group of alkyl, alcenyl, haloalkyl, cycloalky, phenyl or naphtyle, saturated, unstaturated or aromatic heterocycle having from five to six members which contain from one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, or R1 and R2 can from together with a connecting them nitrogen atom a cycle of 5 to 6 members containing from one to four nitrogen atoms or from one to three nitrogen atoms and one sulfur or oxygen atom, R3 is a cycloalkyl or bicycloalkyl group, R1, R2 and R3 can be substituted in conformity with a description, and X is an alkyl or alkyl halide group. The inventive methods and intermediary products necessary for producing said compounds, agents containing them and the use therefore for fighting against harmful mushroom are also disclosed.
本发明涉及式(I)的5-烷基-7-
氨基三唑
嘧啶及其盐。在所述式中,取代基具有以下含义:R1和R2分别是氢原子或烷基、烯基、卤代烷基、环烷基、苯基或
萘基的基团,饱和、不饱和或含有从一到四个氮原子或一个
硫或氧原子的五到六个成员的芳香杂环,或R1和R2可以与连接它们的氮原子一起形成一个含有从一到四个氮原子或一个
硫或氧原子的五到六个成员的环,R3是环烷基或双环烷基,R1、R2和R3可以根据描述被取代,X是烷基或烷基卤化物基团。还公开了制备所述化合物所需的创新方法和中间产物、含有它们的制剂以及用于对抗有害真菌的用途。